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rs1055149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1055149(C;T)
Make rs1055149(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354181
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1055149
ebirs1055149
HLIrs1055149
Exacrs1055149
Varsomers1055149
Maprs1055149
PheGenIrs1055149
hapmaprs1055149
1000 genomesrs1055149
hgdprs1055149
ensemblrs1055149
gopubmedrs1055149
geneviewrs1055149
scholarrs1055149
googlers1055149
pharmgkbrs1055149
gwascentralrs1055149
openSNPrs1055149
23andMers1055149
23andMe allrs1055149
SNP Nexus

SNPshotrs1055149
SNPdbers1055149
MSV3drs1055149
GWAS Ctlgrs1055149
GMAF0.08815
Max Magnitude0
ClinVar
Risk rs1055149(T;T)
Alt rs1055149(T;T)
Reference rs1055149(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31321958G>A
CLNSRC
CLNACC